ANDA 210510

ABHAI LLC

FDA Drug Application

Application #210510

Application Sponsors

ANDA 210510

ABHAI LLC

Marketing Status

• Prescription: 001

Application Products

001

SUSPENSION;ORAL

750MG/5ML

0

ATOVAQUONE

ATOVAQUONE

FDA Submissions

UNKNOWN;

ORIG

1

AP

2019-05-31

STANDARD

Submissions Property Types

ORIG

1

Null

7

TE Codes

001

Prescription

AB

CDER Filings

ABHAI LLC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 210510
            [companyName] => ABHAI LLC
            [docInserts] => ["",""]
            [products] => [{"drugName":"ATOVAQUONE","activeIngredients":"ATOVAQUONE","strength":"750MG\/5ML","dosageForm":"SUSPENSION;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"05\/31\/2019","submission":"ORIG-1","actionType":"Approval","submissionClassification":"","reviewPriority":"STANDARD","inserts":"[]","notes":"> Label is not available on this site."}]
            [supplements] => 
            [actionDate] => 2019-05-31
        )

)